APA aipamena

Jiao, X., Sultana, A., Garg, P., Ramamurthy, B., Vemuganti, G. K., Gangopadhyay, N., . . . Kannabiran, C. (2007). Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. BMJ Group.

Chicago Style aipamena

Jiao, Xiaodong, Afia Sultana, Prashant Garg, Balasubramanya Ramamurthy, Geeta K. Vemuganti, Nibaran Gangopadhyay, J Fielding Hejtmancik, and Chitra Kannabiran. Autosomal Recessive Corneal Endothelial Dystrophy (CHED2) Is Associated With Mutations in SLC4A11. BMJ Group, 2007.

MLA aipamena

Jiao, Xiaodong, et al. Autosomal Recessive Corneal Endothelial Dystrophy (CHED2) Is Associated With Mutations in SLC4A11. BMJ Group, 2007.